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2,5,6-Trichloro-3-trifluoromethylpyridine, a pyridine derivative with the molecular formula C6H2Cl3F3N, is a chemical compound characterized by the presence of three chlorine and three fluorine atoms. It is widely recognized for its role as an intermediate in the synthesis of various agrochemicals and pharmaceuticals, as well as a building block in the production of insecticides, fungicides, and herbicides.

80289-91-4

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80289-91-4 Usage

Uses

Used in Agrochemicals and Pharmaceuticals:
2,5,6-Trichloro-3-trifluoromethylpyridine is used as an intermediate in the synthesis of various agrochemicals and pharmaceuticals due to its unique chemical structure and reactivity. Its presence in these compounds contributes to their effectiveness in controlling pests and diseases in agriculture and treating various medical conditions.
Used in Insecticides:
2,5,6-Trichloro-3-trifluoromethylpyridine is used as a building block in the production of insecticides. Its incorporation into these compounds enhances their ability to target and eliminate harmful insects, thereby protecting crops and reducing the impact of infestations on agricultural yields.
Used in Fungicides:
Similarly, 2,5,6-Trichloro-3-trifluoromethylpyridine is utilized in the development of fungicides. Its presence in these compounds aids in combating fungal infections that can damage crops and reduce their quality and yield.
Used in Herbicides:
2,5,6-Trichloro-3-trifluoromethylpyridine also plays a role in the production of herbicides. Its integration into these compounds helps in controlling the growth of unwanted plants, ensuring optimal crop growth and productivity.
Used in Coatings and Adhesives:
Furthermore, 2,5,6-Trichloro-3-trifluoromethylpyridine is utilized in the manufacturing of materials for coatings and adhesives. Its unique properties contribute to the development of high-performance coatings and adhesives with enhanced durability, adhesion, and resistance to various environmental factors.
It is crucial to handle 2,5,6-Trichloro-3-trifluoromethylpyridine with care, as it may pose potential hazards to health and the environment. Proper safety measures and precautions should be taken during its production, use, and disposal to minimize any adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 80289-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,8 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80289-91:
(7*8)+(6*0)+(5*2)+(4*8)+(3*9)+(2*9)+(1*1)=144
144 % 10 = 4
So 80289-91-4 is a valid CAS Registry Number.

80289-91-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,6-trichloro-5-(trifluoromethyl)pyridine

1.2 Other means of identification

Product number -
Other names 2,3,6-Trichloro-5-trifluoromethyl-pyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80289-91-4 SDS

80289-91-4Relevant academic research and scientific papers

METHOD FOR PREPARING 2,3-DICHLORO-5-TRIFLUOROMETHYLPYRIDINE WITH HIGH SELECTIVITY

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Paragraph 0147; 0161, (2020/04/24)

The present invention discloses a method for preparing 2,3-dichloro-5-trifluoromethylpyridine, comprising at a temperature of 100?150° C. and a pressure of 0.5?5.0 MP, in presence of at least one catalyst selected from supported metal chloride, supported zeolite molecular sieve and supported heteropolyacid, 2-chloro-5-trifluoromethylpyridine reacts with chlorine gas to obtain 2,3-dichloro-5-trifluoromethylpyridine. The preparing method provided by the present invention has advantages such as high selectivity of desired product, high utilization rate of chlorine gas, moderate process condition, simple operation and less three wastes. The present invention also discloses a preparing method for preparing 2-chloro-5-trifluoromethylpyridine, which is capable of reducing unit consumption, reducing separation cost, and improving safety compared to the prior art.

Process for producing 5-chloro-β-trifluoromethylpyridines

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, (2008/06/13)

5,6-Dichloro-β-trifluoromethylpyridine or 2,5,6-trichloro-β-trifluoromethylpyridine is produced by reacting 6-chloro-β-trifluoromethylpyridine or 2,6-dichloro-β-trifluoromethylpyridine with chlorine gas to chlorinate the 5-position of pyridine nucleus thereof: (1) at a temperature of 100° C. to 250° C. and at least sufficient amount of chlorine for the reaction; (2) in the presence of the catalyst of amount of at least 40% by weight (based on the 6-chloro or/and 2,6-dichloro-β-trifluoromethylpyridine), the catalyst being chlorides a metallic element selected from the group consisting of iron, tungsten, molybdenum, titanium, and antimony.

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